Variant #0000858254 (NC_000002.11:g.211457616A>C, NM_001122633.2:c.1118A>C (CPS1))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.211457616A>C
DNA change (hg38) -
Published as CPS1(NM_001875.4):c.1100A>C (p.E367A)
ISCN -
DB-ID CPS1_000311
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2024-08-28 13:07:21 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CPS1 NM_001122633.2 -?/. - c.1118A>C r.(?) p.(Glu373Ala)
CPS1 NM_001875.4 -?/. - c.1100A>C r.(?) p.(Glu367Ala)


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